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Diseases
Genes (1355)
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COL2A1
Collagen, Type Ii, Alpha-1
Cataract
TTPA
Familial Isolated Vitamin E Deficiency
TFAP2A
Branchiooculofacial Syndrome
Cataract
PQBP1
Cataract
Renpenning's Syndrome
UMOD
Medullary Cystic Kidney Disease
SLC20A2
Primary Familial Brain Calcification
PAH
Phenylketonuria
Cataract
PDGFRB
Primary Familial Brain Calcification
MIP
Pleural Effusion
Cataract
EDN1
Auriculocondylar Syndrome 3
Normal Tension Glaucoma
CRYGD
Cataract
IFIH1
Singleton Merten Syndrome
GNAI3
Auriculocondylar Syndrome 3
PLCB4
Auriculocondylar Syndrome 3
ZIC1
Craniosynostosis 1
CCDC50
Deafness, Autosomal Dominant 44
SLC1A1
Normal Tension Glaucoma
PDGFB
Primary Familial Brain Calcification
RB1
Pinealoblastoma
Trilateral Retinoblastoma
Cataract
CRYAA
Cataract